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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2066798Generated: November 1, 2026

N-[5-(bromoacetyl)-4-methyl-1,3-thiazol-2-yl]acetamide → HCID 86649582, compound

https://huagongshe.com/reaction/2066798

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[5-(bromoacetyl)-4-methyl-1,3-thiazol-2-yl]acetamideHCID 19974111—
ReactantHCID 86086574HCID 86086574—
CatalystPhosphomolybdic acidHCID 159350—
SolventMethanolHCID 887—
ProductHCID 86649582HCID 86649582—

Reaction Steps

To a solution of N-[5-(2-bromo-acetyl)-4-methyl-thiazol-2-yl]-acetamide (0.29 g, prepared as described in WO 2005/068444) in MeOH (15 mL) at rt was added 1-trifluoromethyl-cyclopropanecarbothioic acid amide [871913-36-9] (0.20 g) and ammoniumphosphomolybdate (0.15 g). After stirring 18 h at rt, the reaction mixture was partitioned between EtOAc and water, the organic layers dried over Na2SO4 and evaporated to give the crude product. Purification by flash chromatography with an eluent of 1% MeOH in CH2Cl2 gave the title compound. MS (ESI): positive 348.1 (M+H), negative 346.1 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08293753B2
Source datasetuspto-grants-2012_10
ORD IDord-48ec6858d80f43d2ad9d095adb267fe5
Source noteuspto-grants-2012_10